HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52294Erstellt: 24. Oktober 2026
4-Chlorobenzonitrile → 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide
https://huagongshe.com/de/reaction/52294
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Chlorobenzonitrile | HCID 12163 | — |
| Edukt | 4-(Methylsulfonyl)aniline | HCID 79617 | — |
| Edukt | Trimethylaluminum | HCID 16682925 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide | HCID 178504796 | — |
Reaktionsschritte
To a suspension of 4-(methylsulfonyl)aniline (7 g, 41 mmol) in toluene (400 mL), trimethylaluminum (2M solution in toluene, 30.5 mL, 61 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-chlorobenzonitrile (11.3 g, 82 mmol) in toluene (200 mL) was added over 10 minutes and the reaction mixture was heated to 80°-85° C. After 16 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol. The combined filtrates were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 1000 mL). The intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (10.93 g, 86%) was used in the next reaction without further purification: mp (DSC) 191° C. Anal. Calc'd. for C14H13N2SO2Cl: C, 54.46, H, 4.24, N, 9.07. Found: C, 54.42, H, 4.30, N, 9.07.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616601 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-45e2e30cff9d4228995f8b63eba08d26 |
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| Quellennotiz | uspto-grants-1997_04 |
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